rs7412, APOE

N. diseases: 47
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hepatitis E
CUI: C0085293
Disease: Hepatitis E
2 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2018 2018
Cerebral Vasospasm
CUI: C0265110
Disease: Cerebral Vasospasm
3 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2018 2018
response to statin
CUI: C3549252
Disease: response to statin
8 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2012 2012
Hyperlipoproteinemia Type III
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
24 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 0
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2014 2014
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
29 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2016 2016
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.800 1.000 1 2012 2012
Osteopenia
CUI: C0029453
Disease: Osteopenia
61 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2010 2010
Longevity
CUI: C0023980
Disease: Longevity
74 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2019 2019
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2010 2010
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2015 2015
Lipoprotein (a) measurement
CUI: C1096202
Disease: Lipoprotein (a) measurement
103 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2017 2017
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2015 2015
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2017 2017
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1 2010 2010
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2014 2014
Dementia
CUI: C0497327
Disease: Dementia
176 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1 2010 2010
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2010 2010
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2015 2015
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2011 2011
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.030 1.000 3 2014 2019
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2012 2012
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2019 2019
Hepatolenticular Degeneration
CUI: C0019202
Disease: Hepatolenticular Degeneration
349 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2018 2018
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2016 2016